? Cytogenetics Shared Resource The Cytogenetic Shared Resource (CSR) is an SJCCC-managed Shared Resource with the overarching goal of providing Center members with access to high-quality, comprehensive cell-based genetic assays and associated expertise for cancer research. We accomplish this goal by collaborating with SJCCC members to determine project goals and develop and apply customized assays and analysis to advance member research. The CSR is directed by Marcus Valentine, who has more than 35 years of experience in cytogenetics and is a co-author of 90 peer-reviewed scientific articles. He is supported by 2 technologists, each of whom has more than 30 years of experience in the field. Examples of new assays developed in the current project period include assays for identifying the presence of numerous clinically actionable gene-fusion events in ALL (HMP, Roberts et al., NEJM, 2014) and assignment of hundreds of genes to specific epigenetic compartments within the retina (DBSTP, Aldiri et al., Neuron, 2017). The impact of the CSR on the cancer research of the Programs is evidenced by the high level of collaborative publications and key scientific contributions in high-impact journals such as Cancer Cell (n=5), Blood (n=3), and Nature Communications (n=4). During the current funding period, research from 53 publications from January 2013?December 2017 utilized the CSR, representing 15 (28%) interprogrammatic and 18 (34%) intraprogrammatic collaborations. These included publications from 4 of the 5 Programs: DBSTP (n=9), HMP (n=22), CBP (n=19), and NBTP (n=24). During the index year (FY2017), 85% of all investigators using the CSR were SJCCC members (22/26). Goals for the next period include continuing to develop and apply new assays to support the cancer research of SJCCC members in emerging areas such as epigenetics. In addition, to support the precision medicine goals of the SJCCC strategic plan, the CSR will work collaboratively with SJCCC members to develop and validate new assays as new gene rearrangements are discovered, and transfer these assays for implementation in patient diagnostics. Lastly, the CSR will monitor technical improvements in the field (eg., advanced microscopy) that may be appropriate for implementation in the CSR.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA021765-40
Application #
9632008
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2019-03-01
Budget End
2020-02-29
Support Year
40
Fiscal Year
2019
Total Cost
Indirect Cost
Name
St. Jude Children's Research Hospital
Department
Type
DUNS #
067717892
City
Memphis
State
TN
Country
United States
Zip Code
38105
Perez, Giselle K; Kirchhoff, Anne C; Recklitis, Christopher et al. (2018) Mental health insurance access and utilization among childhood cancer survivors: a report from the childhood cancer survivor study. J Cancer Surviv 12:528-536
Oladimeji, Peter O; Chen, Taosheng (2018) PXR: More Than Just a Master Xenobiotic Receptor. Mol Pharmacol 93:119-127
Wilson, Carmen L; Howell, Carrie R; Partin, Robyn E et al. (2018) Influence of fitness on health status among survivors of acute lymphoblastic leukemia. Pediatr Blood Cancer 65:e27286
Mueller, Emily L; Park, Elyse R; Kirchhoff, Anne C et al. (2018) Insurance, chronic health conditions, and utilization of primary and specialty outpatient services: a Childhood Cancer Survivor Study report. J Cancer Surviv 12:639-646
Wong, Timothy; Wang, Zhican; Chapron, Brian D et al. (2018) Polymorphic Human Sulfotransferase 2A1 Mediates the Formation of 25-Hydroxyvitamin D3-3-O-Sulfate, a Major Circulating Vitamin D Metabolite in Humans. Drug Metab Dispos 46:367-379
Triplett, Brandon M; Muller, Brad; Kang, Guolian et al. (2018) Selective T-cell depletion targeting CD45RA reduces viremia and enhances early T-cell recovery compared with CD3-targeted T-cell depletion. Transpl Infect Dis 20:
Crawford, Rebecca R; Potukuchi, Praveen K; Schuetz, Erin G et al. (2018) Beyond Competitive Inhibition: Regulation of ABC Transporters by Kinases and Protein-Protein Interactions as Potential Mechanisms of Drug-Drug Interactions. Drug Metab Dispos 46:567-580
Weil, Brent R; Madenci, Arin L; Liu, Qi et al. (2018) Late Infection-Related Mortality in Asplenic Survivors of Childhood Cancer: A Report From the Childhood Cancer Survivor Study. J Clin Oncol 36:1571-1578
Levine, Jennifer M; Whitton, John A; Ginsberg, Jill P et al. (2018) Nonsurgical premature menopause and reproductive implications in survivors of childhood cancer: A report from the Childhood Cancer Survivor Study. Cancer 124:1044-1052
Li, Jian-Feng; Dai, Yu-Ting; Lilljebjörn, Henrik et al. (2018) Transcriptional landscape of B cell precursor acute lymphoblastic leukemia based on an international study of 1,223 cases. Proc Natl Acad Sci U S A 115:E11711-E11720

Showing the most recent 10 out of 6764 publications